Enhanced generation of leukotriene B-4 and superoxide radical from calciumionophore (A23187) stimulated human neutrophils after priming with interferon-alpha.

Citation
Oa. Al-shabanah et al., Enhanced generation of leukotriene B-4 and superoxide radical from calciumionophore (A23187) stimulated human neutrophils after priming with interferon-alpha., RES COM M P, 106(1-2), 1999, pp. 115-128
Citations number
33
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
RESEARCH COMMUNICATIONS IN MOLECULAR PATHOLOGY AND PHARMACOLOGY
ISSN journal
10780297 → ACNP
Volume
106
Issue
1-2
Year of publication
1999
Pages
115 - 128
Database
ISI
SICI code
1078-0297(1999)106:1-2<115:EGOLBA>2.0.ZU;2-4
Abstract
The present study was designed to investigate the effect of interferon-alph a ( INF-alpha) on the production of leukotrienes (LTs) and superoxide radic als when intact human neutrophils were stimulated with calcium ionophore (A 23187). A reverse phase high performance liquid chromatography and UV spect roscopy were employed to detect and quantitate the released LTs; namely LTC 4, LTB4 and its trans isomers, 6-trans LTB4 and 12-epi-6-trans LTB4 Preincu bation of intact human neutrophils at 37 degreesC for 30 min with INF-alpha and stimulation with calcium ionophore A23187 for 1 min enhanced significa ntly the formation of LTB4. Preincubation of intact human neutrophils with INF-alpha and subsequent stimulation with calcium ionophore A23187 also enh anced significantly superoxide radical generation that reduced nitroblue te trazolium into blue formazan. The in vivo effect of INF-alpha in rats demonstrated that the higher dose o f INF-alpha that induced superoxide radical and LTB4 by A23187 stimulated i ntact human neutrophil in vitro, also induced a significant decrease in whi te blood cells and RBCs started at 4 h after i.p administration. The differ ential white blood cell count revealed that, the prime target for INF-alpha is the white blood cells of myeloid origin. These results might demonstrat e the modulatory effects of INF-alpha, on granulocyte functions.